IP Library Granted Patent US 7,411,104
Granted Patent B2
US 7,411,104 · App. 11/390,880 · Granted Aug 12, 2008

Method for producing polybutene

Assignee: Daelim Industrial Co., Ltd.
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Quick Facts
Patent No.
US 7,411,104
App. No.
11/390,880
Granted
Aug 12, 2008
Kind
B2
Abstract

A method for producing high reactive polybutene (HRPB), in which carbon-carbon double bond is positioned at an end of polybutene, is disclosed. The high reactive polybutene having 300˜5000 of number average molecular weight (Mn) can be produced from a raw material containing isobutene, wherein a polymerization reaction of the isobutene is carried out in the presence of a catalyst system including secondary alkylether, tertiary alcohol, and boron trifluoride, the amount of boron trifluoride is 0.05˜1.0 weight part per 100 weight part of isobutene, the mole ratio of a co-catalyst including secondary alkylether and tertiary alcohol:boron trifluoride is 1.0˜2.0:1, and the mole ratio of secondary alkylether:tertiary alcohol is 0.5˜1.2:1.

Claims (10)

1. A method for producing high reactive polybutene having 300˜5000 of number average molecular weight (Mn) from (a) isobutene, (b) C4 hydrocarbon compounds derived from cracking of naphtha, and containing more than 10 weight % of isobutene, or (c) C4 hydrocarbon compounds derived from a refining process of crude oil or from catalytic cracking of heavy gas oil, and containing more than 10 weight % of isobutene,

wherein a polymerization reaction of the isobutene is carried out in the presence of a catalyst system comprising secondary alkylether, tertiary alcohol, and boron trifluoride, the amount of boron trifluoride is 0.05˜1.0 weight part per 100 weight part of isobutene, the mole ratio of a co-catalyst including secondary alkylether and tertiary alcohol:boron trifluoride is 1.0˜2.0:1, and the mole ratio of secondary alkylether:tertiary alcohol is 0.5˜1.2:1.

2. The method according to claim 1 , wherein the secondary alkylether is selected from the group consisting of diisopropylether, di(sec-butyl)ether, di(sec-hexyl)ether, di(sec-octyl)ether and mixtures thereof.

3. The method according to claim 1 , wherein the tertiary alcohol is selected from the group consisting of t-butylalcohol, 4-hydroxy-4-methyl-2-pentanone, 2-methyl-2-butanol and mixtures thereof.

4. The method according to claim 1 , wherein the polymerization reaction is carried out at the temperature of −50˜20° C.

5. The method according to claim 1 , wherein the catalyst system further includes one or more solvent selected from the group consisting of chloromethane, dichloromethane, and chloroform.

6. A method of producing high reactive polybutene, comprising the steps of:

preparing a catalyst system including secondary alkylether, tertiary alcohol, and boron trifluoride;

introducing the catalyst system to a polymerizing reaction of (a) isobutene, (b) C4 hydrocarbon compounds derived from cracking of naphtha and containing more than 10 weight % of isobutene, or (c) C4 hydrocarbon compounds derived from a refining process of crude oil or from catalytic cracking of heavy gas oil and containing more than 10 weight % of isobutene, to form a polymerization product; and

stripping the polymerization product to generate high reactive polybutene having a 300˜5000 number average molecular weight, wherein the amount of boron trifluoride is 0.05˜1.0 weight part per 100 weight part of isobutene, the mole ratio of a co-catalyst including secondary alkylether and tertiary alcohol:boron trifluoride is 1.0˜2.0:1, and the mole ratio of secondary alkylether:tertiary alcohol is 0.5˜1.2:1.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2021
From: DAELIM INDUSTRIAL CO., LTD.
To: DL CHEMICAL CO., LTD.
Reel/Frame 057189/0449 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2006
From: YUN, HYUN-KI; LIM, BYEONG-GYU; KIM, MYEONG-SEOG; OH, SE-SAENG; UHM, JAE-HOON
To: DAELIM INDUSTRIAL CO., LTD
Reel/Frame 017573/0682 →
Priority Claims (1)
KR 2000-67057 · Nov 13, 2000 · national
Continuity (2)
Continuation In Part 1016954700
Related Publication 20060195000A1 · Aug 31, 2006